Active Ingredient: FOSPHENYTOIN SODIUM
Proprietary Name: FOSPHENYTOIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 50MG PHENYTOIN NA/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078736
Product Number: 001
Approval Date: Jun 8, 2010
Applicant Holder Full Name: PHARMOBEDIENT CONSULTING LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
